S33F (p.Ser33Phe) variant of TNFRSF13B (O14836)
S33F (p.Ser33Phe) in TNFRSF13B (O14836) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
S33F (p.Ser33Phe) variant details
- p.Ser33Phe
- NCI-TCGA Cosmic COSV5542
- cosmic curated COSV55426
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.